EP0069399A2 - Composition pharamceutique contenant des liposomes qui contiennent l'ubidecarenone - Google Patents

Composition pharamceutique contenant des liposomes qui contiennent l'ubidecarenone Download PDF

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Publication number
EP0069399A2
EP0069399A2 EP82106124A EP82106124A EP0069399A2 EP 0069399 A2 EP0069399 A2 EP 0069399A2 EP 82106124 A EP82106124 A EP 82106124A EP 82106124 A EP82106124 A EP 82106124A EP 0069399 A2 EP0069399 A2 EP 0069399A2
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EP
European Patent Office
Prior art keywords
liposome
ubidecarenone
phosphatidyl
coq
pharmaceutical composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP82106124A
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German (de)
English (en)
Other versions
EP0069399A3 (en
EP0069399B1 (fr
Inventor
Masahiro Takada
Teruaki Yuzuriha
Kouichi Katayama
Junzo Sunamoto
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eisai Co Ltd
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Eisai Co Ltd
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Filing date
Publication date
Application filed by Eisai Co Ltd filed Critical Eisai Co Ltd
Publication of EP0069399A2 publication Critical patent/EP0069399A2/fr
Publication of EP0069399A3 publication Critical patent/EP0069399A3/en
Application granted granted Critical
Publication of EP0069399B1 publication Critical patent/EP0069399B1/fr
Expired legal-status Critical Current

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/10—Dispersions; Emulsions
    • A61K9/127—Synthetic bilayered vehicles, e.g. liposomes or liposomes with cholesterol as the only non-phosphatidyl surfactant
    • A61K9/1277—Preparation processes; Proliposomes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/10—Dispersions; Emulsions
    • A61K9/127—Synthetic bilayered vehicles, e.g. liposomes or liposomes with cholesterol as the only non-phosphatidyl surfactant
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/12—Ketones
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/12—Ketones
    • A61K31/122—Ketones having the oxygen directly attached to a ring, e.g. quinones, vitamin K1, anthralin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system

Definitions

  • This invention relates to a ubidecarenone-containing liposome which permits rapid transfer of ubidecarenone from the blood to a target organ, as well as a pharmaceutical composition containing the same.
  • Ubidecarenone also known as coenzyme Q 10 , has recently come into widespread clinical use as a medecine effective for improving the function of the heart.
  • ubidecarenone Since ubidecarenone is a normally solid lipid-soluble substance having a melting point of 48 to 52°C, it must be solubilized by a conventional technique involving the use of a surfactant such as HCO (polyoxyethylene-hardened castor oil) in order to render it convenient for intravenous administration.. However, if it is administered in the thus solubilized state, the speed of disappearance of ubidecarenone from the blood'is low, and the speed of its transfer in the initial stage to the heart, spleen and liver, ie., the target organs, especially to the heart is low.
  • HCO polyoxyethylene-hardened castor oil
  • the present inventors have made various investigations about a ubidecarenone-containing composition which is effective for increasing the transfer of ubidecarenone from the blood to predetermined target organs. These investigations have led to the discovery that such a composition can be provided by incorporating ubidecarenone in liposome.
  • a ubidecarenone-containing liposome there is provided a ubidecarenone-containing liposome.
  • Figure 1 is a graphic representation showing the results obtained in Experimental Example 1 to be given hereinbelow
  • Figures 2 to 4 are graphic representations showing the results obtained in Experimental Example 2 to be given hereinbelow.
  • the liposome itself is known, and a conventional method is available for its production.
  • a ubidecarenone-containing liposome has been produced by applying the liposome technology to ubidecarenone, thereby solving the aforesaid basic problem of ubidecarenone and greatly increasing the utilitarian value of ubidecarenone.
  • ubidecarenone is contained in a membrane constituting the liposome.
  • the liposome is composed basically of a phospholipid and a sterol. Ubidecarenone is present together with these substances and dispersed uniformly within the membrane.
  • Examples of the phospholipid.used in this invention are phosphatidyl choline, phosphatidyl ethanolamine, phosphatidyl serine, sphingomyelin, dicetylphos phoric acid, stearylamine, phosphatidyl glycerol, phosphatidic acid, phosphatidyl inositol and mixtures thereof. It is however not specifically limited to these exemplified species. On the other hand, cholesterol is most preferred as the sterol.
  • the proportions of ubidecarenone, the phospholipid and the sterol in the liposome are preferably such that at least 10 moles of the phospholipid and- at least 1 mole of the sterol are present per mole of ubidecarenone.
  • the proportion of the phospholipid is preferably 10 to 30 moles,if it is egg yolk phosphatidyl choline, and the proportion of the sterol is preferably 1 to 10 moles, if it is cholesterol.
  • the liposome of this invention when observed under an electron microscope, is a spherical particle having a particle diameter' of about 0.1 to 5.0 ⁇ m. Its lyophilized product is aggregated and in appearance it is the form of a block. When put into water or salt solutions, it disperses well to give a homogeneous solution.
  • the liposome of this invention can be produced substantially in accordance with the conventional technique for the production of liposome.
  • it can be produced by charging a membrane-constituting component of the liposome and ubidecarenone into an eggplant-shaped flask, adding chloroform to dissolve these substances, then evaporating the solvent, peeling the resulting membrane by adding a glass bead and a suitable buffer etc., ultrasonicating the resulting solution, passing the treated solution through a column of Sephadex or Sepharose, collecting liposome fractions, and removing the solvent.
  • the removal of the solvent can be effected by, for example, lyophilization.
  • the lyophilization is carried out for at least 3 hours. under a pressure of not more than 2.0 torr, the intended object of this invention can be achieved and the liposome can be taken out as a powder.
  • the invention is not limited to these specific conditions.
  • the lyophilization is desirably carried out for 5 hours under a pressure of 0.3 torr, for example.
  • the invention also comprises a pharmaceuitcal composition, which contains the ubidecarenone-containing liposome according to the invention besides usual pharmaceutically acceptable carriers and/or diluents.
  • Liposome was prepared by the same method as described in Example 1 except that 14 C-CoQ 10 was used instead of CoQ 10 described in Example 1. The resulting liposome was used as an assay sample. A control sample was obtained by adding HCO-60. to 14 C-CoQ 10 , the amount of the former being four times that of the latter, and subjecting the solution to ultrasonication, and adding physiological saline to a concentration of 0.6 mg/ml.
  • the assay sample was injected in an amount of 0.6 mg as 14 C-CoQ 10 /kg into the left femoral vein of male guinea pigs (body weight 300 - 350 g).
  • the control sample was administered in the same dose by the same method.
  • the animals were then left in a cage, and every predetermined period of time, blood was drawn from the ear vein.
  • the concentration of 14 C-CoQ 10 in the blood was measured by the following method.
  • the curve marked by o refers to the case of administering the assay sample (average of two runs), and the curve marked by to the case of administering the control sample (an average of 3 runs, and a standard deviation);
  • the disappearance of 14 C-CoQ 10 in the assay sample from the blood is indicated by two straight lines which are bent at 1 hour after the administration. The half-life period of its disappearance is 11.5 minutes in the first phase and 15.6 hours in the second phase.
  • the disappearance of 14 C-CoQ 10 in the control sample from the blood is indicated by one straight line, and the half-life period of its disappearance is 20.1 hours. It is seen from these results that the-disappearance of 14 C-CoQ 10 in the assay sample from the blood is much more rapid than that of 14 C-CoQ 10 in the control sample.
  • Each of the above samples was injected in a dose of 0.6 mg/kg into the left femoral vein of male guinea pigs (body weight 300 g - 350 g). The animals were then left in a cage. Thirty minutes and 24 hours respectively after the administration, the animals were killed by decapitation, and the organs were removed. In order to prevent contamination of the brain and heart by blood, physiological saline was circulated from the left ventricle to the jugular vein to draw the blood, and then the brain and heart were removed.
  • the hatched columns refer to the case of administering the assay sample (an average of 2 runs), and the blank columns ⁇ , to the case of administering the control sample (an average of 3 runs, and a standard deviation, provided that in the case of the results obtained 30 minutes after the administration with regard to the brain and heart, the indicated values are averages of 2 runs).
  • the distribution of 14 C-CoQ 10 to the tissues its concentration increased more rapid-ly, and lasted longer, in the assay sample than in the control sample.
  • the distribution of the assay sample differs from that of the control sample.
  • 14 C-CoQ 10 In regard to the transfer of 14 C-CoQ 10 to the brain, heart, liver, spleen and adrenal gland, it was distributed more rapidly in higher concentrations in the case of the assay sample than in the case of the control sample. It was specifically found that 30 minutes after the administration, 14 C-CoQ 10 in the assay sample was distributed in the heart in a concentration 16 times as high as that in the control sample and in the brain 2 times as high as that in the control sample.
  • the solution was then transferred to a branched test tube, and subjected to ultrasonication treatment at 42W for 53 minutes intermittently every 30 seconds by using a probe-type sonicator in an ice bath under a stream of argon to give a translucent pale yellow solution.
  • the solution was applied onto a column (1.6 x 45 cm) of Sepharose 4B, and eluted with the buffer A. Then, 1.8 ml portions of the eluate were taken respectively into 60 test tubes. A fraction which was eluted near the void volume of this column was concentrated .to a final volume of 1.7 ml (0.55 mg as CoQ 10 ) by means of a polycarbonate membrane having a pore size of 0.08 ⁇ m. The resulting liposome had a diameter of 80 to 100 ⁇ m by observation under an electron microscope.
  • the buffer A denotes a 0.01M phosphate buffer (pH 7.4) containing 0.1M NaCl.
  • a 200 ml eggplant-shaped flask was charged with 60.0 mg (3 moles) of yolk phosphatidyl choline, 9.8 mg (1 mole) of cholesterol and 6.5 mg (0.3 moles) of ubidecarenone, and 4 ml of chloroform was added to dissolve them.
  • the solvent was evaporated under reduced pressure.
  • Four milliliters of physiological saline and a glass bead were added, and dispersed by using a vortex mixer.
  • the resulting multilayer film was transferred to a branched test tube, and under an atmosphere of nitrogen gas, subjected to ultrasonication treatment at 25 KW for 15 minutes in an ice bath.
  • the solution was then charged onto a column of Sephadex G-50 and eluted with physiological saline as an eluent. Liposome fractions were collected and diluted to 30 ml. The diluted liposome fractions were lyophilized for 5 hours under a pressure of 0.3 torr.

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Epidemiology (AREA)
  • Dispersion Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Preparation (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
EP82106124A 1981-07-08 1982-07-08 Composition pharamceutique contenant des liposomes qui contiennent l'ubidecarenone Expired EP0069399B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP105689/81 1981-07-08
JP56105689A JPS588010A (ja) 1981-07-08 1981-07-08 ユビデカレノン含有リポソ−ム

Publications (3)

Publication Number Publication Date
EP0069399A2 true EP0069399A2 (fr) 1983-01-12
EP0069399A3 EP0069399A3 (en) 1983-03-30
EP0069399B1 EP0069399B1 (fr) 1986-10-29

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ID=14414361

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EP82106124A Expired EP0069399B1 (fr) 1981-07-08 1982-07-08 Composition pharamceutique contenant des liposomes qui contiennent l'ubidecarenone

Country Status (7)

Country Link
EP (1) EP0069399B1 (fr)
JP (1) JPS588010A (fr)
KR (1) KR880002036B1 (fr)
CA (1) CA1197463A (fr)
DE (1) DE3273949D1 (fr)
ES (1) ES8401526A1 (fr)
PH (1) PH17553A (fr)

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1988003015A1 (fr) * 1986-10-23 1988-05-05 Arval S.P.A. Preparation cosmetique contenant des ubidecarenones
WO1988003019A1 (fr) * 1986-10-23 1988-05-05 Vincenzo Zappia Derives hydrosolubles d'ubidecarenones et leur preparation
US5204108A (en) * 1987-10-10 1993-04-20 Danbiosyst Uk Ltd. Transmucosal formulations of low molecular weight peptide drugs
EP0494654A3 (en) * 1991-01-09 1993-05-19 Kanegafuchi Kagaku Kogyo Kabushiki Kaisha Stable pharmaceutical composition and method for its production
US5690954A (en) * 1987-05-22 1997-11-25 Danbiosyst Uk Limited Enhanced uptake drug delivery system having microspheres containing an active drug and a bioavailability improving material
AU688033B2 (en) * 1994-07-06 1998-03-05 Colgate-Palmolive Company, The Aqueous liquid detergent compositions containing deflocculating polymers
WO2002090304A1 (fr) * 2001-05-09 2002-11-14 Kaneka Corporation Solution stable de coenzyme q reduite
US6726924B2 (en) * 1997-09-04 2004-04-27 Biozone Laboratories, Inc. Oral liposomal delivery system
WO2004082668A1 (fr) * 2003-03-20 2004-09-30 Shanghaijahwa United Co., Ltd. Proliposome contenant la coenzyme q10 et son procede de preparation
US20100062048A1 (en) * 2006-05-02 2010-03-11 University Of Miami Topical co-enzyme q10 formulations and treatment of pain, fatigue and wounds
WO2011112900A2 (fr) 2010-03-12 2011-09-15 Cytotech Labs, Llc Formulations intraveineuses de coenzyme q10 (coq10) et leurs procédés d'utilisation
US11419830B2 (en) 2017-05-17 2022-08-23 Berg Llc Use of coenzyme Q10 formulations in the treatment and prevention of epidermolysis bullosa

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6132789A (en) * 1995-12-15 2000-10-17 National Research Council Of Canada Archaeosomes, archaeosomes containing coenzyme Q10, and other types of liposomes containing coenzyme Q10 as adjuvants and as delivery vehicles
DE10255285A1 (de) * 2002-11-26 2004-06-03 Mcs Micro Carrier Systems Gmbh Selbst formende Phospholipid-Gele
JP2006137684A (ja) * 2004-11-10 2006-06-01 Nippon Fine Chem Co Ltd リポソーム前駆体の製造方法
JP5140913B2 (ja) * 2005-09-14 2013-02-13 日油株式会社 コエンザイムｑ１０含有化粧料用リポソーム

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2249552A1 (de) * 1971-10-12 1973-05-30 Inchema S A Verfahren zur inkapsulation von insbesondere wasserloeslichen verbindungen
JPS5919527B2 (ja) * 1976-01-13 1984-05-07 バテル メモリアル インステイチユ−ト リポソ−ムの製造方法
JPS5356315A (en) * 1976-11-01 1978-05-22 Eisai Co Ltd Emulsified solution of fat soluble drugs
JPS55118415A (en) * 1979-02-28 1980-09-11 Pii Papahadojiyopo Dometoriosu Method of encapsulating biologically active substance in lipoid cell
FR2472384A1 (fr) * 1979-12-27 1981-07-03 Sederma Sa Utilisation en cosmetologie de complexes naturels constitues d'ubiquinones et de phospholipides

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1988003015A1 (fr) * 1986-10-23 1988-05-05 Arval S.P.A. Preparation cosmetique contenant des ubidecarenones
WO1988003019A1 (fr) * 1986-10-23 1988-05-05 Vincenzo Zappia Derives hydrosolubles d'ubidecarenones et leur preparation
US5690954A (en) * 1987-05-22 1997-11-25 Danbiosyst Uk Limited Enhanced uptake drug delivery system having microspheres containing an active drug and a bioavailability improving material
US5204108A (en) * 1987-10-10 1993-04-20 Danbiosyst Uk Ltd. Transmucosal formulations of low molecular weight peptide drugs
EP0494654A3 (en) * 1991-01-09 1993-05-19 Kanegafuchi Kagaku Kogyo Kabushiki Kaisha Stable pharmaceutical composition and method for its production
US5298246A (en) * 1991-01-09 1994-03-29 Kanegafuchi Kagaku Kogyo Kabushiki Kaisha Stable pharmaceutical composition and method for its production
AU688033B2 (en) * 1994-07-06 1998-03-05 Colgate-Palmolive Company, The Aqueous liquid detergent compositions containing deflocculating polymers
US6726924B2 (en) * 1997-09-04 2004-04-27 Biozone Laboratories, Inc. Oral liposomal delivery system
WO2002090304A1 (fr) * 2001-05-09 2002-11-14 Kaneka Corporation Solution stable de coenzyme q reduite
WO2004082668A1 (fr) * 2003-03-20 2004-09-30 Shanghaijahwa United Co., Ltd. Proliposome contenant la coenzyme q10 et son procede de preparation
US20100062048A1 (en) * 2006-05-02 2010-03-11 University Of Miami Topical co-enzyme q10 formulations and treatment of pain, fatigue and wounds
US10583098B2 (en) * 2006-05-02 2020-03-10 Sung Lan Hsia Topical co-enzyme Q10 formulations and treatment of pain, fatigue and wounds
WO2011112900A2 (fr) 2010-03-12 2011-09-15 Cytotech Labs, Llc Formulations intraveineuses de coenzyme q10 (coq10) et leurs procédés d'utilisation
EP3366280A1 (fr) 2010-03-12 2018-08-29 Berg LLC Préparations intraveineuses de coenzyme q10 (coq10) et leurs procédés d'utilisation
US11419830B2 (en) 2017-05-17 2022-08-23 Berg Llc Use of coenzyme Q10 formulations in the treatment and prevention of epidermolysis bullosa
US12616666B2 (en) 2017-05-17 2026-05-05 Bpgbio, Inc. Coenzyme Q10 formulations in the treatment and prevention of epidermolysis bullosa

Also Published As

Publication number Publication date
EP0069399A3 (en) 1983-03-30
EP0069399B1 (fr) 1986-10-29
KR880002036B1 (ko) 1988-10-13
JPH0321525B2 (fr) 1991-03-22
ES513789A0 (es) 1983-12-16
JPS588010A (ja) 1983-01-18
PH17553A (en) 1984-09-20
KR840000241A (ko) 1984-02-18
ES8401526A1 (es) 1983-12-16
CA1197463A (fr) 1985-12-03
DE3273949D1 (en) 1986-12-04

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